Effectiveness and Safety of Electro-acupuncture for Mild-to-moderate Perimenopausal Depression

Sponsor
Guangdong Provincial Hospital of Traditional Chinese Medicine (Other)
Overall Status
Unknown status
CT.gov ID
NCT02423694
Collaborator
(none)
252
1
2

Study Details

Study Description

Brief Summary

Main objective: to compare the effects of electro-acupuncture and escitalopram oxalate tablets on mild-to-moderate perimenopausal depression, and to evaluate the safety of electroacupuncture stimulation.

Condition or Disease Intervention/Treatment Phase
  • Device: electro-acupuncture
  • Drug: escitalopram oxalate tablets
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
252 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Study Start Date :
Sep 1, 2013
Anticipated Primary Completion Date :
Dec 1, 2015

Arms and Interventions

Arm Intervention/Treatment
Experimental: Electroacupuncture

Baihui, Yintang, Guanyuan(dual), Zigong(dual), Sanyinjiao(dual), Hegu(dual), Taichong(dual). Insert needles to the acupoints mentioned above after sterilized.Needle handles of Baihui and Yintang are connected with the electroacupuncture instrument wire. And needle handles of bilateral Zigong are conneted with the electroacupunture instrument wire. And needle handles of bilateral Tianshu are connected with the electroacupunture instrument wire. Density wave, frequency of 10/50Hz and current intensity is 0.5~1.0 mA for 30 minutes. 3 times per week. Each treatment interval of more than 24 hours, continuous treatment for 12 weeks.

Device: electro-acupuncture
8 acupoint: Guanyuan, Zigong (bilateral), Tianshu(bilateral), Sanyinjiao(bilateral), Hegu(bilateral), Taichong(bilateral), Baihui, Yintang. Every patient is supposed to have 36 times acupuncture treatment. 30 minutes per time. Baihui, Yintang, Zigong (bilateral), Tianshu (bilateral) are applied with electro-acupuncture device with dilatational wave, current frequency: 10/50Hz, intensity: 0.5~1.0 mA

Active Comparator: escitalopram oxalate tablets

0.5 hour after breakfast oral taking 10mg escitalopram oxalate tablets, continuous treatment for 12 weeks.

Drug: escitalopram oxalate tablets
escitalopram oxalate tablet, once a day, 0.5 hour after breakfast, oral taken, 10mg, for 12 weeks

Outcome Measures

Primary Outcome Measures

  1. Change from Baseline in scores of the 17-item Hamilton depression rating scale (HAMD-17) [0 week, 4th week, 8th week, 12th week, 16th week and 24th week]

Secondary Outcome Measures

  1. Change from Baseline in scores of the Menopause-Specific Quality of Life questionnaire (MENQOL) [0 week, 4th week, 8th week, 12th week, 16th week, 20th week and 24th week]

  2. Change from Baseline in level of estradiol (E2), [0 week, 12th week]

  3. Change from Baseline in level of follicle-stimulating hormone (FSH) [0 week, 12th week]

  4. Change from baseline in level of Luteinizing hormone (LH) [0 week, 12th week]

  5. Change from baseline in level of FSH/LH [0 week, 12th week]

Other Outcome Measures

  1. safety of electro-acupuncture as measured by safety and acceptability questionnaires [0 week, 4th week, 8th week, and 12th week]

    safety and acceptability

  2. safety of escitalopram as measured by Asberg Rating Scale for Side Effect (SERS) [0 week, 4th week, 8th week, and 12the week]

    Asberg Rating Scale for Side Effect (SERS)

  3. safety of escitalopram as measured by liver functure test [0 week, 4th week, 8th week, and 12the week]

    ALT, aspartate transminase (AST), and TBIL

  4. safety of escitalopram as measured by kidney functure test [0 week, 4th week, 8th week, and 12the week]

    Cr, BUN

  5. safety of both groups before treatment as measured by EKG [0 week]

    EKG

  6. safety of both groups before treatment as meausred by blood regular test [0 week]

    Blood regular test

  7. safety of both groups before treatment as measured by urine regular test [0 week]

    Urine regular test

Eligibility Criteria

Criteria

Ages Eligible for Study:
45 Years to 55 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Conforms to the diagnosis standard of STRAW-10 for perimenopause, conforms to the diagnosis standard of The Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) for depression, and conforms to the diagnosis standard of The International Statistical Classification of Diseases and Related Health Problems 10th Revision (ICD-10) F32.0(mild depression) or F32.1(moderate depression);

  • Fisrt attack during perimenopausal period;

  • HAMD-17 score >7 and <23;

  • Age ≥45 to ≤55;

  • No hormone replacement therapy (HRT) or no antidepressant 3 months before into the group;

  • Sign the consent consent, volunteered for this study

Exclusion Criteria:
  • Fail to rule out the possibility of suicide in depression factor of The Symptom Checklist (SCL-90);

  • Application of estrogen, progesterone, selective serotonin reuptake inhibitors (SSRIs), soybean isoflavone, vitamin E or black cohosh in recent 4 weeks;

  • Allergic to citalopram or escitalopram tablets;

  • Taken the non selective, irreversible inhibitor of monoamine oxidase (MAOIs) in recent 2 weeks;

  • Taken linezolid, pimozide, tryptophane,tramadol, triptans or other drugs that may cause drug adverse reactions in recent 2 weeks;

  • Patient with prolongation of the QT interval or congenital long QT syndrome

  • Taken herbs or products that contain isatin, pilose antler, hawthorn, fleeceflower root, common St.John's wort herb, hypericin;

  • Ovarian dropsy or hysteromyoma with more than 4cm diameter, oophorectomy, or hysterectomy;

  • Mandatory indications of hormonotherapy, such as surgery-induced menopause or osteoporosis;

  • Patient with history of radiotherapy or chemotherapy, or undergoing radiotherapy or chemotherapy;

  • Vaginal bleeding of undetermined origin;

  • Patient with coagulation disorders, or taking anticoagulants such as Warfarin, or heparin;

  • Patient with skin diseases, such as eczema,or psoriasis;

  • Serious hepatic insufficiency or serious renal inadequacy;

  • Uncontrolled hypertension, diabetes, or thyroid disease;

  • Diabetic neuropathy, or malignant tumor;

  • Pregnancy intention, in pregnancy or lactation;

  • Regular use of sedative and anti anxiety drugs;

  • The long-term smoking and/or drinking;

  • Having Pacemaker or artificial joint;

  • Electrolyte is disorder, serious heart disease or other potential life-threatening disease patients;

  • Compliance may be poor or fear of acupuncture.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Guangdong Provincial Hospital of Traditional Chinese Medicine Guangzhou Guangdong China 510120

Sponsors and Collaborators

  • Guangdong Provincial Hospital of Traditional Chinese Medicine

Investigators

  • Study Chair: Wenbin Fu, MD, Guangdong Provincial Hospital of Traditional Chinese Medicine

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Fu Wenbin, Professor, Guangdong Provincial Hospital of Traditional Chinese Medicine
ClinicalTrials.gov Identifier:
NCT02423694
Other Study ID Numbers:
  • 2012BAI24B01
First Posted:
Apr 22, 2015
Last Update Posted:
Apr 22, 2015
Last Verified:
Apr 1, 2015
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 22, 2015